Functional characterization of the copper transcription factor AfMac1 from Aspergillus fumigatus

Yong Sung Park, Tae Hyoung Kim, Cheol Won Yun

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27 Citations (Scopus)


Although copper functions as a cofactor in many physiological processes, copper overload leads to harmful effects in living cells. Thus, copper homeostasis is tightly regulated. However, detailed copper metabolic pathways have not yet been identified in filamentous fungi. In this report, we investigated the copper transcription factor AfMac1 (Aspergillus fumigatus Mac1 homolog) and identified its regulatory mechanism in A. fumigatus. AfMac1 has domains homologous to the DNA-binding and copper-binding domains of Mac1 from Saccharomyces cerevisiae, and AfMac1 efficiently complemented Mac1 in S. cerevisiae. Expression of Afmac1 resulted in CTR1 up-regulation, and mutation of the DNA-binding domain of Afmac1 failed to activate CTR1 expression in S. cerevisiae. The Afmac1 deletion strain of A. fumigatus failed to grow in copper-limited media, and its growth was restored by introducing ctrC. We found that AfMac1 specifically bound to the promoter region of ctrC based on EMSA. The AfMac1-binding motif 50-TGTGCTCA-30 was identified from the promoter region of ctrC, and the addition of mutant ctrC lacking the AfMac1-binding motif failed to up-regulate ctrC in A. fumigatus. Furthermore, deletion of Afmac1 significantly reduced strain virulence and activated conidial killing activity by neutrophils and macrophages. Taken together, these results suggest that AfMac1 is a copper transcription factor that regulates cellular copper homeostasis in A. fumigatus.

Original languageEnglish
Pages (from-to)2365-2378
Number of pages14
JournalBiochemical Journal
Issue number14
Publication statusPublished - 2017 Jul 15

Bibliographical note

Funding Information:
This work was supported by a National Research Foundation of Korea (NRF) grant funded by the Korea Government Ministry of Science, Information & Communication Technology (ICT) and Future Planning (MSIP) [No. NRF-2014R1A2A1A11050920] and was supported by a Korea University Grant.

Publisher Copyright:
© 2017 The Author(s); published by Portland Press Limited on behalf of the Biochemical Society.

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology


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